Serum Lipids in Turkish Patients with β-Thalassemia Major and β-Thalassemia Minor
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چکیده
Conflict of Interest: The authors of this paper have no conflicts of interest, including specific financial interests, relationships, and/or affiliations relevant to the subject matter or materials included. References 1. Harteveld CL, Higgs DR. Alpha-thalassaemia. Orphanet J Rare Dis 2010;5:13. 2. Blackwell RQ, Jim RT, Tan TG, Weng MI, Liu CS, Wang CL. Hemoglobin G Waimanalo: alpha-64 Asp leads to Asn. Biochim Biophys Acta 1973;322:27-33. 3. Brennan SO, Chan T, Ryken S, Ruskova A. A second case of Hb Fontainebleau [alpha21(B2)Ala-->Pro] in an individual with microcytosis. Hemoglobin 2009;33:258-261. 4. Akar N. An updated review of abnormal hemoglobins in the Turkish population. Turk J Hematol 2014;31:97-98. 5. Lin M, Wu JR, Yang LY, Chen H, Wang PP, Wang Q, Zheng L. Hb G-Waimanalo: occurrence in combination with alpha-thalassemia-1 Southeast Asian deletion. Blood Cells Mol Dis 2009;42:36-37. 6. Tan TG, Jim RT, Blackwell RQ. Hemoglobin G Waimanalo beta thalassemia. Hawaii Med J 1978;37:235-239. 7. Lin M, Wang Q, Zheng L, Huang Y, Lin F, Lin CP, Yang LY. Prevalence and molecular characterization of abnormal hemoglobin in eastern Guangdong of southern China. Clin Genet 2012;81:165-171. 8. Wajcman H, Blouquit Y, Gombaud-Saintonge G, Riou J, Galacteros F.Hb Fontainebleau [alpha 21(B2)Ala----pro], a new silent mutant hemoglobin. Hemoglobin 1989;13:421-428. 9. Turner A, Sasse J, Varadi A. Hb Fontainebleau (HBA2: c.64G > C) in the United Arab Emirates. Hemoglobin 2014;38:216-220.
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